Bovilis Vista BVD CFP (Canada)

Bovine Virus Diarrhea Vaccine

Modified Live Virus

Cattle Vaccine

Bovilis Vista BVD CFP Indications

This product has been shown to be effective for the vaccination of healthy cattle, 3 months of age or older against respiratory disease and fetal infection, including persistently infected calves due to bovine virus diarrhea virus (BVD) Types 1 & 2. Respiratory duration of immunity is at least 1 year and reproductive duration of immunity is at least 206 days. For more information regarding efficacy and safety data, see productdata.aphis.usda.gov.

SAFETY: Safe for use in pregnant heifers and cows or calves nursing pregnant cows provided the cows and heifers in the herd are vaccinated prior to breeding, within the previous 12 months, with any of the modified live BVD containing vaccine(s) in this product line. Calves vaccinated before the age of 6 months should be revaccinated after 6 months of age or at weaning. Prior to use of this vaccine during pregnancy and consistent with good vaccination practices, it is recommended that cows and heifers receive for primary vaccination at least 2 doses of a modified live BVD containing vaccine(s) in this product line, with the second dose given at or about 30 days prior to breeding.

MIXING DIRECTIONS: 10 Doses - Rehydrate freeze dried vial with accompanying vial of diluent. Mix reconstituted vial well.

50 Doses - Rehydrate freeze dried vial with part of the accompanying vial of diluent using the transfer needle provided (see below for pictorial directions). Mix reconstituted vial well and transfer rehydrated vaccine into diluent vial using transfer needle. Remove transfer needle from the former diluent vial and mix reconstituted vial well. Peel label from the vaccine vial and place on diluent vial containing all vaccine.

DOSAGE: Shake well and administer a 2 mL dose aseptically by the subcutaneous route. For advice on revaccination frequency, contact your veterinarian.

Mixing Instructions

CAUTION: THE TRANSFER NEEDLE, INCLUDED IN THE CARTON PACKAGING (50 DOSES), IS SHARP AND MAY CAUSE INJURY TO SELF OR ANIMALS IF NOT HANDLED OR DISPOSED OF PROPERLY.

1. Insert the transfer needle fully into the small vial of dehydrated vaccine to release the vacuum.

2. Insert the other end of the transfer needle fully into the large vial of sterile diluent.

3. Squeeze enough diluent from the large bottle into the smaller vial to rehydrate the vaccine.

4. With the two bottles still attached, swirl the small vial gently until the vaccine is mixed.

5. With the small vial upside down, squeeze the large bottle several times to draw the mixed vaccine into the large bottle.

6. Separate the bottles and remove the vaccine label from the small vial and apply it to the large bottle for proper identification.

Bovilis Vista BVD CFP Caution

Store at 2 to 8°C (35 to 46°F). Fetal health risks associated with the vaccination of pregnant animals with this vaccine cannot be unequivocally determined during clinical trials conducted for licensure. Appropriate strategies to address the risks associated with vaccine use in pregnant animals should be discussed with a veterinarian. Use entire contents when first opened. Do not use chemical disinfectants to sterilize syringes or needles. Do not mix with other products, except as specified on the label. Dispose of containers and all unused vaccine according to local biohazardous waste disposal regulations. Do not vaccinate within 21 days of slaughter. Anaphylactoid reactions may occur following use. Antidote: Epinephrine. Contains Penicillin and Streptomycin as a preservative. In case of human exposure, contact a physician.

FOR ANIMAL USE ONLY

Intervet Inc. d/b/a Merck Animal Health, Omaha, NE 68103

VLN 165A

For patent information:

http://www.merck.com/product/patent/home.html

1 866 683-7838

CPN: 1208330.0